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1H-Pyrrole-2,5-dione, 1-methyl-3-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

716-00-7

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716-00-7 Usage

Chemical class

Pyrroles It belongs to the class of pyrroles, which are heterocyclic aromatic compounds.

Ring structure

Five-membered ring with one nitrogen atom The compound has a five-membered ring structure that includes one nitrogen atom, making it a heterocyclic compound.

Derivative of pyrrole-2,5-dione

1-methyl-3-(4-methylphenyl)1H-Pyrrole-2,5-dione, 1-methyl-3-(4-methylphenyl)- is derived from pyrrole-2,5-dione by attaching a methyl group at the 1-position and a 4-methylphenyl group at the 3-position.

Methyl group

1-position A methyl group (CH3) is attached to the first position of the pyrrole ring.

4-Methylphenyl group

3-position A 4-methylphenyl group (C6H4-CH3) is attached to the third position of the pyrrole ring.

Application

Pharmaceutical and research field The compound is commonly used in the pharmaceutical and research fields, particularly for the development of new drugs and bioactive molecules.

Unique structure and properties

The compound's structure and properties make it an interesting target for chemical synthesis and biological studies.

Check Digit Verification of cas no

The CAS Registry Mumber 716-00-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 716-00:
(5*7)+(4*1)+(3*6)+(2*0)+(1*0)=57
57 % 10 = 7
So 716-00-7 is a valid CAS Registry Number.

716-00-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-(4-methylphenyl)pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-2,5-dione,1-methyl-3-(4-methylphenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:716-00-7 SDS

716-00-7Relevant academic research and scientific papers

Approach to the Synthesis of Unsymmetrical/Symmetrical Maleimides via Desulfitative Arylation at Different Temperatures

Abbasnia, Masoumeh,Sheykhan, Mehdi,Ghaffari, Tahereh,Safari, Elham

, p. 11688 - 11698 (2020/10/23)

New routes toward selective synthesis of both mono-and diaryl maleimides have been innovated. The mere requirement to this end is through the increase of temperature. The method works effectively for maleic anhydride and maleic acid as well. Also, the fir

Diels-Alder Dimerization of 2-Arylmaleimides. X-Ray Crystal Structure of the Dimer of 2-p-Tolylmaleimide

Epstein, Joseph W.,McKenzie, Thomas C.,Lovell, M. F.,Perkinson, Nancy A.

, p. 314 - 315 (2007/10/02)

Dimers (4) and (7) were obtained during the course of the Meerwein arylation reaction; a Diels-Alder reaction is proposed for the mechanism of the dimerization, and the X-ray structure of (4) is reported.

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